Canonical Allele Identifier: CA129831382

Gene: IL12B

Linked Data

• dbSNP Id: rs909354457
• gnomAD v3: 5-159327032-G-C
• gnomAD v4: 5-159327032-G-C
• MyVariant Identifiers: chr5:g.158754040G>C (hg19) ; chr5:g.159327032G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.159327032G>C , CM000667.2:g.159327032G>C	GRCh38
NC_000005.9:g.158754040G>C , CM000667.1:g.158754040G>C	GRCh37
NC_000005.8:g.158686618G>C	NCBI36
NG_009618.1:g.8442C>G , LRG_71:g.8442C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000696750.1:c.-149+3400C>G	ENSP00000512849.1:n.-149+3400C>G
ENST00000696751.1:c.1-250C>G	ENSP00000512850.1:n.1-250C>G
ENST00000696752.1:n.433-250C>G
ENST00000231228.3:c.1-250C>G MANE Select	ENSP00000231228.2:n.1-250C>G
ENST00000231228.2:c.1-250C>G	ENSP00000231228.2:n.1-250C>G
NM_002187.2:c.1-250C>G , LRG_71t1:c.1-250C>G	NP_002178.2:n.1-250C>G
NM_002187.3:c.1-250C>G MANE Select	NP_002178.2:n.1-250C>G